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Catalytic Advantages of SO 3 H-Modified UiO-66(Zr) Materials Obtained via Microwave Synthesis in Friedel-Crafts Acylation Reaction.

Marta BauzaPedro LeoCarlos Palomino CabelloAntonio MartinGisela OrcajoGemma Turnes PalominoFernando Martínez
Published in: Inorganic chemistry (2024)
The catalytic activity and stability of sulfonic-based UiO-66(Zr) materials were tested in the Friedel-Crafts acylation of anisole with acetic anhydride. The materials were prepared using microwave-assisted synthesis, producing microporous materials with remarkable crystallinity and physicochemical features as acid catalysts. Different ratios between both organic ligands, terephthalic acid (H 2 BDC) and monosodium 2-sulfoterephthalic acid (H 2 BDC-SO 3 Na), were used for the synthesis to modulate the sulfonic content. The sulfonic-based UiO-66(Zr) material synthesized with a H 2 BDC/H 2 BDC-SO 3 Na molar ratio of 40/60 exhibited the best catalytic performance in the acidic-catalyzed Friedel-Crafts acylation reaction. This ratio balanced the number of sulfonic acid sites and their accessibility within the UiO-66 microporous structure. The catalytic performance of this material increased remarkably at 200 °C, outperforming reference acids and commercial heterogeneous catalysts such as Nafion-SAC-13 and Amberlyst-70. Additionally, the best sulfonic-based UiO-66(Zr) material proved to be stable in four successive reaction cycles, maintaining both its catalytic activity and its structural integrity.
Keyphrases
  • metal organic framework
  • pet imaging
  • highly efficient
  • computed tomography
  • crystal structure
  • ionic liquid
  • electron transfer